Teva Pharmaceuticals USA is the leading generic pharmaceutical company, marketing products from a wide range of therapeutic areas including cardiovascular, anti-infective, CNS, anti-inflammatory, oncolytic, antidiabetic, analgesic, dermatology, respiratory, and female healthcare. Dosage forms include tablets and capsules, injectables, creams, ointments, inhalants, solutions, and suspensions. Teva USA products are marketed to chains, wholesalers, distributors and government agencies, as well as in health systems and oncology settings.

Teva USA has an aggressive Research and Development effort and one of the best overall ANDA approval records in the industry. The company's mission is to play a leading role in the transformation of the U.S. healthcare system through its pre-eminence in the development, manufacture and marketing of generic pharmaceuticals.

Overview:

Teva Pharmaceuticals is the leading global generic pharmaceutical company employing 26,000 people worldwide. The company's aggressive growth strategy has positioned Teva as a top 20 global pharmaceutical company with plans to be Top 10 in the coming years. Teva is the largest manufacturer and distributor of pharmaceuticals in the world.

Teva USA is a wholly-owned subsidiary of Teva Pharmaceutical Industries Ltd., Israel's largest pharmaceutical manufacturer operating globally in 19 countries on 5 continents. Teva Pharmaceuticals USA is looking for a Publishing Specialist for the Regulatory Operations group at our Woodcliff, NJ location. This exciting opportunity will be part of a team of specialists providing submission ready structure in CTD/eCTD format for all Regulatory submissions to the FDA.

Responsibilities:

Responsibilities may include:

• Creating Hyperlinks/Cross-References/Bookmarks
• Using technical expertise to become lead for eCTD submissions
• Troubleshooting document issues with MSWord
• Management of all technical aspects for assigned submissions and status updates to concerned parties
• Collaborations with scientific personnel for planning, preparation, publishing, and quality control checks of submissions
• Fielding publishing/process questions from other business units
• Maintaining expert knowledge of internal and external publishing standards

Qualifications:

This position requires a Bachelors Degree in Life Sciences or Information Technology and a minimum of 2 years relevant experience in publishing regulatory submissions with industry accredited software solutions. Prior experience with Documentum, Adobe Acrobat, and CoreDossier are highly preferred but may be waived with a strong technical background and experience if one of the above requirements are satisfied.

The candidate must exhibit excellent interpersonal, communication, organizational and follow-up skills. The candidate must also demonstrate personal initiative, responsibility, flexibility, the ability to work under limited supervision, and be able to handle multiple project assignments.

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Search Firm Representatives Please Read Carefully:

Teva is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails.

All resumes submitted by search firms to any employee at Teva via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Teva. No fee will be paid in the event the candidate is hired by Teva as a result of the referral or through other means.